JPH0350979Y2 - - Google Patents

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Publication number
JPH0350979Y2
JPH0350979Y2 JP1983106534U JP10653483U JPH0350979Y2 JP H0350979 Y2 JPH0350979 Y2 JP H0350979Y2 JP 1983106534 U JP1983106534 U JP 1983106534U JP 10653483 U JP10653483 U JP 10653483U JP H0350979 Y2 JPH0350979 Y2 JP H0350979Y2
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Japan
Prior art keywords
resin
weight
talc
liquid sample
container
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Expired
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JP1983106534U
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Japanese (ja)
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JPS6017240U (en
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  • Containers Having Bodies Formed In One Piece (AREA)
  • Devices For Use In Laboratory Experiments (AREA)

Description

【考案の詳細な説明】 本考案は、耐水性,耐薬品性が良好であつて、
易焼却性の液体試料用容器に関する。 各種の化学実験,水質試験などにおける液体試
料用容器としては従来よりガラス製ビーカーが最
も一般的に用いられている。また、病院等におい
ても検尿などの目的で各種液体試験を採取するた
めの容器が使用されている。 近年、これらに用いられる容器類として、洗浄
を合理化するために、使い捨て容器として紙製,
合成樹脂製あるいは紙と合成樹脂からなる積層物
製のものが多く用いられている。しかしながら、
紙製コツプは軽量で焼却性にすぐれているが、耐
水性に劣るため液体試料用容器としてはほとんど
使用されていない。そこで、紙に合成樹脂をコー
テイングもしくはラミネートした積層物が紙に代
る容器素材として提案された。この積層物により
耐水性はある程度改善されるが、積層体の製造工
程のほか紙製容器の場合と同じく容器の製造にあ
たり接着工程を要するため、生産性が低い上に接
着部分を有するため、安全性の面でも問題があつ
た。 このため、ポリスチレン,ポリオレフインなど
の合成樹脂製の容器が広く用いられている。しか
し、これらの合成樹脂製の容器は加工性,軽量
性,衛生性などに優れているが、廃棄焼却に際し
て燃焼カロリーが紙に比べて大幅に高く、焼却炉
の炉壁を傷めたり、溶融固化を生じるなどの欠点
がある。また、表面が滑らかなため採取試料名な
どを鉛筆書きすることができず、さらに軽量のた
め安定性に欠けると共に強度,剛性,耐溶剤性,
耐熱性等も十分でなく、使用分野が大きく制限さ
れている。 そこで、本考案者らは燃焼カロリーが低く、耐
水性,耐薬品性,耐熱性,強度等が良好であつ
て、表面に鉛筆書きが可能で、かつ安定感のある
液体試料用の容器を開発すべく鋭意研究した結
果、特定の材料を用いて得られる容器が目的を満
足するものであるという知見を得、本考案を完成
した。 すなわち本考案は、ポリプロプレン系樹脂とポ
リエチレン系樹脂との混合物からなり、かつ、そ
の混合比が、ポリプロピレン系樹脂:ポリエチレ
ン系樹脂=7:3〜3:7(重量比)であるポリ
オレフイン系樹脂に対し、平均粒径5〜30μのタ
ルクを組成物全体の20〜70重量%および酸化チタ
ンを組成物全体の1〜10重量%の割合で配合せし
めてなるポリオレフイン系樹脂材料よりなる液体
試料用容器である。 本考案におけるポリオレフイン系樹脂は、上記
の如く、ポリプロプレン系樹脂とポリエチレン系
樹脂との混合物からなるものである。 ここでポリプロピレン系樹脂としては、プロピ
レンのホモポリマーやプロピレンと30重量%以下
のエチレンなど他のα−オレフインとのブロツク
コポリマーやランダムコポリマーなど、さらには
これらの混合物などがある。また、このポリプロ
ピレン系樹脂のメルトインデツクスは、一般に
0.1〜5g/10分、好ましくは0.2〜3g/10分、
より好ましくは0.3〜1.5g/10分のものである。
この場合において、メルトインデツクスが5g/
10分を越えるものでは、シートの溶融強度が小さ
く、逆に0.1g/10分未満のものでは流動性が悪
く、タルクとの均一混練性が充分でなく、共に熱
成形などの二次成形性が困難となる。 一方、ポリエチレン系樹脂についても様々なも
のがあり、例えば高密度ポリエチレン,中密度ポ
リエチレン,低密度ポリエチレンなどがあげら
れ、エチレンのホモポリマーのほか、エチレンと
30重量%以下の他のα−オレフイン(プロピレン
など)とのランダムあるいはブロツクコポリマー
がある。ここで高密度ポリエチレンとしては密度
0.940〜0・970g/cm3のもの、中・低密度ポリエ
チレンとしては高圧法ポリエチレンや中・低圧法
で得られるエチレンとプロピレン,ブテン−1,
4−メチルペンテン−1,オクテン−1など炭素
数3〜12のα−オレフインとのコポリマー、いわ
ゆる直鎖状低密度ポリエチレン(LLDPE)があ
る。また、このポリエチレン系樹脂のメルトイン
デツクスは、通常は0.02〜10.0g/10分、好まし
くは0.03〜5.0g/10分、より好ましくは0.04〜
2.0g/10分である。このポリエチレン系樹脂の
メルトインデツクスが上記範囲外であると、溶融
混練シート成形性,熱成形などの二次成形性の点
で好ましくない。 本考案においては、軽量の深物容器を真空成形
や圧空成形などの二次成形により連続多量生産を
行なうために、上述のようにポリプロピレン系樹
脂とポリエチレン系樹脂の混合物を用いている。
この混合物におけるポリプロピレン系樹脂とポリ
エチレン系樹脂の混合比は、前者:後者=7:3
〜3:7(重量比)とされる。 次に、本考案におけるタルクは、その種類など
について特に制限されないが、平均粒径が5〜
30μ、好ましくは10〜20μの含水ケイ酸マグネシ
ウムであり、その組成はSiO250〜65%、MgO25
〜40%および他の成分よりなると共に灼熱減量1
%以下のものである。このタルクの配合割合は組
成物全体の20〜70重量%、好ましくは30〜60重量
%の範囲で定める。タルクの配合量が多すぎると
剛性,焼却性は向上するが、溶融混練やシート成
形性さらには熱成形などの二次成形性が低下す
る。 また、タルクとしては前述したように種々のも
のを使用することが可能であり、例えば高度に精
製されたもの、あるいは酸処理されて不純物など
を除去したものを用いることもできる。なお、こ
のタルクは特に表面処理などの付加的手段は必要
としない。 さらに本考案においては酸化チタンを用いる。
ここで酸化チタンは、通常二酸化チタン(TiO2
を指称するが、これに少量の一酸化チタン
(TiO)や三酸化二チタン(Ti2O3)の混入した
ものを用いても差支えない。また、この酸化チタ
ンの形状等については特に制限はないが、一般に
平均粒子径0.05〜2μ、好ましくは0.1〜1μ程度の
粒状,粉末状などである。この酸化チタンを加え
る場合、その配合割合はたとえば組成物から厚さ
1mmのシートを成形した場合、このシートの全光
線透過率が3%以下、特に2%以下になるように
割合を目安とすることが好ましく、具体的には、
組成物全体の1〜10液体試料用容器が適当であ
る。 本考案の液体試料用容器は上記ポリオレフイン
系樹脂,タルクおよび酸化チタンの3成分を素材
とするが、必要により顔料、不飽和カルボン酸ま
たはその誘導体で変性したポリオレフインなどの
樹脂,ゴム,常用の添加剤等を配合することがで
きる。 上記のポリオレフイン系樹脂,タルク,酸化チ
タンおよび所望成分を通常の混練法、すなわちロ
ール,バンバリーミキサー,一軸押出機,多軸押
出機などで十分混練後、カレンダー法,T−ダイ
法などによつてシートに成形する。 次に、このようにして得られたポリオレフイン
系樹脂シートを真空成形,圧空成形などの二次熱
成形によつて液体試料用容器を成形する。この成
形法の採用により、一度に多数個取りができ、成
形サイクルも短かく、連続的に多量生産が可能で
ある。なお、シートの厚みは通常0.2〜3mmであ
る。 さらに、本考案の液体試料用容器はその高さ/
平均径が0.8〜2.0、より好ましくは1.0〜1.8のも
のである。本考案の容器は上述した如く、ポリオ
レフイン系樹脂,タルクおよび酸化チタンからな
るポリオレフイン系樹脂シートを熱成形してなる
ものであるため、溶融混練性を低下させることが
なく、溶融強度も十分であつて深物容器が得られ
る。したがつて、上記範囲の高さ/平均径を有
し、液体試料用容器として好適な容器が得られ
る。なお、容器の形状に関しては円筒状のほか容
器の底部から開口部に向けて拡開させてもよく、
さらに容器の底部周縁にアンダーカツトを設けて
も良い。 このようにして得られた液体試料用容器は次の
ようなすぐれた特性を有している。 すなわち易焼却性で、焼却に際して燃焼カロ
リーが低いため、炉壁の損傷がなく、また溶融固
化を生ずることがない。高い強度を有し、かつ
剛性,耐熱性,耐水性,耐薬品性が良好である。
表面に鉛筆書きでき、表面筆記性が良好であ
る。比重が大きく安定性がある。無臭である
とともにタルクの溶出がなく、液体試料への影響
が少ない。隠ぺい力が高い。生産性に優れて
いる。 したがつて、本考案の液体試料用容器はビーカ
ー代用容器,検尿容器等の各種の使い捨て可能な
液体試料用の容器として有効に利用されることが
期待される。 次に、本考案を実施例により説明する。 実施例 1 ポリプロピレンホモポリマー(密度0.91g/
cm3,メルトインデツクス(MI)0.6g/10分)25
重量%,高密度ポリエチレン(密度0.964g/cm3
MI0.4g/10分)25重量%,平均粒径15μのタル
ク46重量%および酸化チタン4重量%をバンバリ
ーミキサーを用いて溶融混練しペレツト化した
後、押出成形機を用いて厚み1mmのシートを得
た。次いで、圧空成形機(圧力6Kg/cm2)を用い
てカツプ状熱成形品(高さ90mm/平均径60mm=
1.5)を製造した。得られた液体試料用容器は第
1図に示した形状のものであり、底部の厚みが
0.85mm,底部のASTM D 1003による光線透過
率が0.6%であり、周縁部の厚みが0.36mm,該周
縁部の光線透過率が6.3%であつた。この液体試
料用容器の外観はすぐれた高級紙様の風合を有
し、高級感に満ちたものであつた。この液体試料
用容器の座屈強さは19.5Kg,側面圧縮強さは145
gであり、また容器外面の白色度は94.3%,光沢
度GS(60゜)は6.0%であつた。 なお、この液体試料用容器に25℃の水を入れて
から10分経過後の座屈強さは18.5Kg,側面圧縮強
さは160gであつた。また、95℃の熱湯中に10分
間浸漬してもまつたく異常はみられなかつた。こ
の液体試料用容器の燃焼カロリーは5430ca/
gで、HIPS製カツプの9860ca/gと比較して
非常に低く、紙カツプの4500ca/gに近かつ
た。 実施例2〜7および比較例1〜6 実施例1において、各成分の配合割合とタルク
の平均粒径とについて、第1表に示すものとした
こと以外は、実施例1と同様にしてカツプ状熱成
形品(液体試料用容器)を製造し、物性を評価し
た。なお、物性の評価中、座屈強さと側面圧縮強
さによつて、ある程度剛性の評価を行なうことが
できる。 【表】
[Detailed description of the invention] The invention has good water resistance and chemical resistance,
This invention relates to an easily incinerated liquid sample container. Glass beakers have traditionally been most commonly used as containers for liquid samples in various chemical experiments, water quality tests, etc. Containers for collecting various liquid tests for purposes such as urinalysis are also used in hospitals and the like. In recent years, containers made of paper and disposable containers have been introduced to streamline cleaning.
Those made of synthetic resin or a laminate made of paper and synthetic resin are often used. however,
Paper cups are lightweight and have excellent incineration properties, but are rarely used as containers for liquid samples because of their poor water resistance. Therefore, laminates made of paper coated or laminated with synthetic resin have been proposed as an alternative container material to paper. This laminate improves water resistance to some extent, but in addition to the manufacturing process of the laminate, it requires an adhesion process to manufacture the container, just like paper containers, resulting in low productivity and the presence of adhesive parts, making it safe. There were also problems with sexuality. For this reason, containers made of synthetic resins such as polystyrene and polyolefin are widely used. However, although these synthetic resin containers have excellent processability, light weight, and hygiene, they burn significantly more calories than paper when incinerating waste, and they may damage the incinerator wall or melt and solidify. There are disadvantages such as causing In addition, because the surface is smooth, it is impossible to write the name of the collected sample with a pencil, and because it is lightweight, it lacks stability and has poor strength, rigidity, and solvent resistance.
It also lacks sufficient heat resistance, which greatly limits its field of use. Therefore, the present inventors developed a container for liquid samples that burns low calories, has good water resistance, chemical resistance, heat resistance, strength, etc., allows writing on the surface with a pencil, and has a sense of stability. As a result of intensive research, they found that a container made of a specific material satisfies the purpose, and completed the invention. That is, the present invention provides a polyolefin resin which is made of a mixture of polypropylene resin and polyethylene resin, and whose mixing ratio is polypropylene resin: polyethylene resin = 7:3 to 3:7 (weight ratio). On the other hand, for liquid samples made of a polyolefin resin material, which is made by blending talc with an average particle size of 5 to 30μ in a proportion of 20 to 70% by weight of the entire composition and titanium oxide in a proportion of 1 to 10% by weight of the whole composition. It is a container. As mentioned above, the polyolefin resin in the present invention is a mixture of polypropylene resin and polyethylene resin. Examples of the polypropylene resin include propylene homopolymers, block copolymers and random copolymers of propylene and 30% by weight or less of other α-olefins such as ethylene, and mixtures thereof. In addition, the melt index of this polypropylene resin is generally
0.1 to 5 g/10 minutes, preferably 0.2 to 3 g/10 minutes,
More preferably, it is 0.3 to 1.5 g/10 minutes.
In this case, the melt index is 5g/
If the melting time exceeds 10 minutes, the melt strength of the sheet will be low, while if it is less than 0.1g/10 minutes, the fluidity will be poor, and the uniform kneading ability with talc will not be sufficient, resulting in poor secondary formability such as thermoforming. becomes difficult. On the other hand, there are various types of polyethylene resins, such as high-density polyethylene, medium-density polyethylene, and low-density polyethylene.
There are random or block copolymers with up to 30% by weight of other α-olefins (such as propylene). Here, the density of high-density polyethylene is
0.940 to 0.970 g/cm 3 , medium- and low-density polyethylenes include high-pressure polyethylene, ethylene and propylene obtained by medium- and low-pressure methods, butene-1,
There is a so-called linear low density polyethylene (LLDPE), which is a copolymer with an α-olefin having 3 to 12 carbon atoms such as 4-methylpentene-1 and octene-1. The melt index of this polyethylene resin is usually 0.02 to 10.0 g/10 minutes, preferably 0.03 to 5.0 g/10 minutes, and more preferably 0.04 to 10.0 g/10 minutes.
It is 2.0g/10 minutes. If the melt index of the polyethylene resin is outside the above range, it is unfavorable in terms of melt-kneading sheet formability and secondary formability such as thermoforming. In the present invention, a mixture of polypropylene resin and polyethylene resin is used as described above in order to continuously produce large quantities of lightweight deep containers by secondary forming such as vacuum forming and pressure forming.
The mixing ratio of polypropylene resin and polyethylene resin in this mixture is former: latter = 7:3
~3:7 (weight ratio). Next, although the type of talc used in the present invention is not particularly limited, it has an average particle size of 5 to 5.
30μ, preferably 10-20μ hydrated magnesium silicate, its composition is SiO2 50-65%, MgO25
Burning weight loss 1 with ~40% and other ingredients
% or less. The blending ratio of this talc is determined in the range of 20 to 70% by weight, preferably 30 to 60% by weight of the entire composition. If the amount of talc is too large, the rigidity and incineration properties will improve, but the melt kneading, sheet formability, and secondary formability such as thermoforming will deteriorate. Furthermore, as described above, various types of talc can be used, and for example, highly purified talc or talc treated with acid to remove impurities can also be used. Note that this talc does not require any additional means such as surface treatment. Further, in the present invention, titanium oxide is used.
Here, titanium oxide is usually titanium dioxide (TiO 2 )
However, it may also be mixed with a small amount of titanium monoxide (TiO) or dititanium trioxide (Ti 2 O 3 ). The shape of the titanium oxide is not particularly limited, but it is generally in the form of granules or powder with an average particle size of about 0.05 to 2 μm, preferably about 0.1 to 1 μm. When adding this titanium oxide, the mixing ratio should be such that, for example, when a 1 mm thick sheet is formed from the composition, the total light transmittance of this sheet is 3% or less, especially 2% or less. It is preferable that, specifically,
Containers for 1 to 10 liquid samples of the entire composition are suitable. The liquid sample container of the present invention is made of the above three components: polyolefin resin, talc, and titanium oxide, but if necessary, resins such as polyolefin modified with pigments, unsaturated carboxylic acids or derivatives thereof, rubber, and commonly used additives are used. Agents, etc. can be blended. The above polyolefin resin, talc, titanium oxide and desired components are thoroughly kneaded using a normal kneading method, that is, a roll, a Banbury mixer, a single screw extruder, a multi-screw extruder, etc., and then by a calender method, a T-die method, etc. Form into a sheet. Next, the thus obtained polyolefin resin sheet is formed into a liquid sample container by secondary thermoforming such as vacuum forming or pressure forming. By adopting this molding method, many pieces can be molded at once, the molding cycle is short, and continuous mass production is possible. Note that the thickness of the sheet is usually 0.2 to 3 mm. Furthermore, the liquid sample container of the present invention has a height/
The average diameter is 0.8 to 2.0, more preferably 1.0 to 1.8. As mentioned above, the container of the present invention is made by thermoforming a polyolefin resin sheet made of polyolefin resin, talc, and titanium oxide, so it does not reduce melt kneading properties and has sufficient melt strength. A deep container is obtained. Therefore, a container having a height/average diameter within the above range and suitable as a liquid sample container can be obtained. Regarding the shape of the container, it may be cylindrical or may expand from the bottom of the container toward the opening.
Furthermore, an undercut may be provided around the bottom edge of the container. The liquid sample container thus obtained has the following excellent properties. That is, it is easily incinerated and burns a low calorie when incinerated, so there is no damage to the furnace wall and no melting and solidification. It has high strength and good rigidity, heat resistance, water resistance, and chemical resistance.
You can write on the surface with a pencil, and the surface has good writing properties. It has a high specific gravity and is stable. It is odorless, does not elute talc, and has little effect on liquid samples. High concealment power. Excellent productivity. Therefore, it is expected that the liquid sample container of the present invention will be effectively used as a variety of disposable liquid sample containers such as beaker substitute containers and urinalysis containers. Next, the present invention will be explained with reference to examples. Example 1 Polypropylene homopolymer (density 0.91g/
cm 3 , melt index (MI) 0.6g/10min) 25
Weight%, high density polyethylene (density 0.964g/ cm3 ,
MI0.4g/10min) 25% by weight, 46% by weight of talc with an average particle size of 15μ, and 4% by weight of titanium oxide were melt-kneaded using a Banbury mixer to form pellets, and then made into a 1mm thick sheet using an extrusion molding machine. I got it. Next, a cup-shaped thermoformed product (height 90mm/ average diameter 60mm=
1.5) was manufactured. The resulting liquid sample container has the shape shown in Figure 1, with a bottom thickness of
The thickness of the bottom part was 0.85 mm, and the light transmittance according to ASTM D 1003 was 0.6%, and the thickness of the peripheral part was 0.36 mm, and the light transmittance of the peripheral part was 6.3%. The external appearance of this liquid sample container had the texture of high-quality paper and was full of luxury. The buckling strength of this liquid sample container is 19.5Kg, and the side compressive strength is 145
The whiteness of the outer surface of the container was 94.3%, and the glossiness GS (60°) was 6.0%. Note that the buckling strength was 18.5 kg and the side compressive strength was 160 g 10 minutes after filling the liquid sample container with water at 25°C. Furthermore, no abnormality was observed even after immersing the sample in boiling water at 95°C for 10 minutes. The calorie burn of this liquid sample container is 5430ca/
g, which was very low compared to 9860ca/g for HIPS cups and close to 4500ca/g for paper cups. Examples 2 to 7 and Comparative Examples 1 to 6 Cups were prepared in the same manner as in Example 1, except that the blending ratio of each component and the average particle size of talc were as shown in Table 1. A shaped thermoformed product (liquid sample container) was manufactured and its physical properties were evaluated. In addition, during the evaluation of physical properties, rigidity can be evaluated to some extent by buckling strength and side compressive strength. 【table】

座屈強さを示す。
*4:光沢度GS(60°)の数値
Indicates buckling strength.
*4: Glossiness GS (60°) value

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本考案による液体試料容器の1例を示
す断面図である。
FIG. 1 is a sectional view showing an example of a liquid sample container according to the present invention.

Claims (1)

【実用新案登録請求の範囲】[Scope of utility model registration request] ポリプロプレン系樹脂とポリエチレン系樹脂と
の混合物からなり、かつ、その混合比が、ポリプ
ロピレン系樹脂:ポリエチレン系樹脂=7:3〜
3:7(重量比)であるポリオレフイン系樹脂に
対し、平均粒径5〜30μのタルクを組成物全体の
20〜70重量%および酸化チタンを組成物全体の1
〜10重量%の割合で配合せしめてなるポリオレフ
イン系樹脂材料よりなる液体試料用容器。
It is made of a mixture of polypropylene resin and polyethylene resin, and the mixing ratio is polypropylene resin: polyethylene resin = 7:3 ~
Talc with an average particle size of 5 to 30μ is added to the polyolefin resin at a ratio of 3:7 (weight ratio) to the entire composition.
20-70% by weight of titanium oxide and 1% of the total composition
A liquid sample container made of a polyolefin resin material mixed in a proportion of ~10% by weight.
JP10653483U 1983-07-11 1983-07-11 Liquid sample container Granted JPS6017240U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10653483U JPS6017240U (en) 1983-07-11 1983-07-11 Liquid sample container

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10653483U JPS6017240U (en) 1983-07-11 1983-07-11 Liquid sample container

Publications (2)

Publication Number Publication Date
JPS6017240U JPS6017240U (en) 1985-02-05
JPH0350979Y2 true JPH0350979Y2 (en) 1991-10-31

Family

ID=30249270

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10653483U Granted JPS6017240U (en) 1983-07-11 1983-07-11 Liquid sample container

Country Status (1)

Country Link
JP (1) JPS6017240U (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9484824B2 (en) 2005-08-26 2016-11-01 Power Integrations, Inc. Method and apparatus for digital control of a switching regulator

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5250051B2 (en) * 1974-02-05 1977-12-21

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9484824B2 (en) 2005-08-26 2016-11-01 Power Integrations, Inc. Method and apparatus for digital control of a switching regulator

Also Published As

Publication number Publication date
JPS6017240U (en) 1985-02-05

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